The neurological complications of Behcet's syndrome have not been character
ized with clarity. We present the clinical features, imaging characteristic
s and CSF findings of a series of 50 patients seen at the National Hospital
for Neurology and Neurosurgery over the past 10 years. In this series, vas
cular complications had a low prevalence, whereas involvement of the brains
tem was common; spinal cord lesions, hemisphere lesions and meningoencephal
itis also occurred. Optic neuropathy, vestibulocochlear and peripheral nerv
e involvement occurred, but were rare. The prognosis for recovery was in ge
neral good, and the majority of those followed-up over a median of 3 years
(range 1-19 years) had only single attacks. One-third of patients underwent
further attacks, and four underwent progressive deterioration leading to d
isability. Factors suggesting a poor prognosis are repeated attacks, incomp
lete recovery, progressive disease course and a high level of CSF leucocyto
sis during acute attack. These data should be of help in the further defini
tion of the clinical characteristics of this rare neurological disorder and
in the planning of treatment trials.